The mitochondrium provides the energy for the cell - Adenosine Trisphosphate (ATP).
Mitochondria are bounded by two membranes: a smooth outer one,and an inner one which is thrown into folds called cristae.
The endoplasmic reticulum is thought to be a single internal membrane that ramifies throughout the cytoplasm enclosing a single internal space (lumen), which may represent more than 10% of the cell volume. The ER occurs in two morphologically distinct forms - smooth (or agranular) endoplasmic reticulum (SER) and rough (or granular) endoplasmic reticulum (RER). The lumen of the RER is continuous with that of the SER.
Rough-endoplasmic reticulum - rER
The outer membrane of the rER is studded with ribosomes. This gives a basophilic staining to cytoplasm in H&E stains (due to the RNA content). The rER plays a major role in protein synthesis. It synthesises secretory proteins, and lysosomal enzymes.
Cells active in secretion will have lots of rER - and you can see this as purplish staining in the otherwise pink cytoplasm (H&E).
The lining of the smooth endoplasmic reticulum is smooth, has no ribosomes, and has branched tubules. It plays a major role in lipid biosynthesis (makes lipids and steroids) and in detoxification mechanisms.
An electron micrograph showing golgi stacks.
The Golgi apparatus is usually found close to the cell nucleus and consists of one or more stacks of membrane-bound cisternae (sacs). The lumens of these cisternae are separate from each other and from that of the ER.
The Golgi receives synthetic products from the ER, modifies them, and exports them to a variety of destinations. Membrane proteins are collected, sorted and packaged to required destination. For example, secreted proteins are packaged into secretory vesicles and exocytosed. It also produces enzymes that are sorted into lysosomes, to degrade proteins and organelles. It also plays a role in retrieving and recycling proteins.
It has two 'faces' - the cis (receiving or forming or entry) face, and the trans (or maturing or exit) face:
The pathways of endocytosis and exocytosis, are pathways by which proteins are taken up and secreted.
This photograph is a cell that has been fluorescently labelled to show the trans Golgi network (in red). The cell outline has been drawn in, in white. Scale bar - 20 µm.
Secretory vesicles: These are vesicles that can be seen leaving the trans face of the Golgi.
Lysosomes - tiny spherical vesicles (0.2 to 0.4 µm diameter), with an acidic internal PH (ph5.0)- for degrading proteins. Primary lysosomes are produced by the Golgi apparatus. They form secondary lysosomes by fusing with other membrane-bound vesicles in the cytoplasm. These vesicles may contain extracellular material that has entered the cell by phagocytosis and require digesting, or organelles that require degrading (such as in the picture below) because they have reached the end of their active life. They contain around 40 different types of hydrolytic enzymes, including proteases, nucleases and lipases (they are all acid hydrolases, which need an acid pH to work optimally). This process is also used for degrading internal organelles in a process called 'autophagy' - in which cell organelles are marked for destruction. Lysosomes fuse with the organelles to form secondary lysosomes.
What organelle is being digested by the secondary lysosome shown in picture above?
Lysosomes are important for breaking down proteins. There are several 'lysosomal' storage diseases, where a mutation in one of the lysosomal enzymes means that it does not work properly, and proteins can accumulate in lysosomes as they cannot be digested. An example is Hurler's disease, in which an enzyme which breaks down glycosoaminoglycans is missing, and lysosomes accumulate in massive quantities.
Endosomes - endocytic vesicles formed after endocytosis.
Peroxisomes - derived from rough ER, that contain enzymes that will form hydrogen peroxide - which phagocytic cells use to kill bacteria.